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放射性诱发的胶质瘤:4例报告及分子生物标志物分析

Radiation-induced gliomas: a report of four cases and analysis of molecular biomarkers.

作者信息

Nakao Tsunehito, Sasagawa Yasuo, Nobusawa Sumihito, Takabatake Yasushi, Sabit Hemragul, Kinoshita Masashi, Miyashita Katsuyoshi, Hayashi Yasuhiko, Yokoo Hideaki, Nakada Mitsutoshi

机构信息

Division of Neuroscience, Department of Neurosurgery, Graduate School of Medical Science, Kanazawa University, 13-1 Takara-machi, Kanazawa, 920-8641, Japan.

Department of Human Pathology, Gunma University Graduate School of Medicine, Gunma, Japan.

出版信息

Brain Tumor Pathol. 2017 Oct;34(4):149-154. doi: 10.1007/s10014-017-0292-x. Epub 2017 Aug 9.

Abstract

Radiation-induced glioma (RIG) is a rare secondary glioma. The tumors morphologically resemble their sporadically arising counterparts. Recently, the WHO classification of tumors of the central nervous system was revised to incorporate molecular biomarkers together with classic histological features. The status of molecular biomarkers in RIG, however, remains unclear. The objective of this study was to investigate if commonly accepted glioma-specific biomarkers are relevant in RIGs. Among 269 gliomas diagnosed as WHO grade 2, 3 and 4 in our institution, four were diagnosed as RIGs. Immunohistochemical (IHC) staining for isocitrate dehydrogenase 1 (IDH1), p53, alpha thalassemia/mental retardation syndrome X-linked (ATRX), and H3K27M, and direct DNA sequencing of IDH1/2, telomerase reverse transcriptase (TERT) promoter, Histone H3.3 (H3F3A) and B-Raf (BRAF) genes was performed. All tumor specimens were IDH1-, p53- and H3K27M-negative. The nuclei of tumor cells in all cases exhibited positive staining for ATRX. In direct DNA sequencing analysis, no IDH1, IDH2, TERT promoter, H3F3A or BRAF mutations were found in any of the cases. Our findings suggest that these characteristic glioma-associated molecular mutations may be rare events in RIGs. More RIGs need to be tested for analysis of molecular biomarkers to clarify the clinical and histopathological spectra of this tumor.

摘要

放射性诱导胶质瘤(RIG)是一种罕见的继发性胶质瘤。这些肿瘤在形态学上与散发性出现的同类肿瘤相似。最近,世界卫生组织(WHO)对中枢神经系统肿瘤的分类进行了修订,将分子生物标志物与经典组织学特征相结合。然而,RIG中分子生物标志物的状况仍不清楚。本研究的目的是调查公认的胶质瘤特异性生物标志物在RIG中是否相关。在我们机构诊断为WHO 2级、3级和4级的269例胶质瘤中,有4例被诊断为RIG。对异柠檬酸脱氢酶1(IDH1)、p53、α地中海贫血/智力发育迟缓综合征X连锁(ATRX)和H3K27M进行免疫组织化学(IHC)染色,并对IDH1/2、端粒酶逆转录酶(TERT)启动子、组蛋白H3.3(H3F3A)和B-Raf(BRAF)基因进行直接DNA测序。所有肿瘤标本IDH1、p53和H3K27M均为阴性。所有病例中肿瘤细胞核均显示ATRX染色阳性。在直接DNA测序分析中,所有病例均未发现IDH1、IDH2、TERT启动子、H3F3A或BRAF突变。我们的研究结果表明,这些特征性的胶质瘤相关分子突变在RIG中可能是罕见事件。需要对更多的RIG进行分子生物标志物分析检测,以明确该肿瘤的临床和组织病理学特征。

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